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2-Phenylhexane is an aromatic hydrocarbon. It can be produced by a Friedel-Crafts alkylation between 1-chlorohexane and benzene ., [ 1 ] or by the reaction of benzene and 1-hexene with various acid catalysts such as antimony pentafluoride , [ 2 ] scandium(III) triflate , [ 3 ] and phosphoric acid .
2,5-Dimethylhexane; 3,3-Dimethylhexane; 3,4-Dimethylhexane [Wikidata This page was last edited on 27 April 2022, at 16:52 (UTC). Text is available under the ...
9 – MgBr with acetone to form 2,3-dimethyl-2-pentanol, then dehydrating this alcohol to form 2,3-dimethyl-2-pentene, and hydrogenating this product. [ 4 ] The isomer is present at about 2.4% by weight in the hydrocarbon mixture obtained by the condensation of methanol at 200 °C with a zinc iodide catalyst (the main component of the mixture ...
2,3-Dimethylhexane is a structural isomer of octane. References This page was last edited on 27 February 2023, at 20:24 (UTC). Text is available under the Creative ...
Theoretically 2-methylhexane also burns with a less sooty flame, emitting higher-frequency radiation; however, as heptane and 2-methylhexane differ by only one carbon atom, in terms of branching, both burn with a bright yellow flame when ignited. Compared to n-heptane, 2-methylhexane also has lower melting and boiling points. A lower density of ...
ch 2 =ch 2 + ch 3 ch=chch 3 → 2 ch 2 =chch 3 Transition metal catalyzed hydrovinylation is another important alkene synthesis process starting from alkene itself. [ 31 ] It involves the addition of a hydrogen and a vinyl group (or an alkenyl group) across a double bond.
CH 3 (CH 2) 5 COOH heptanedioic acid: pimelic acid: HOOC(CH 2) 5 COOH cyclohexanecarboxylic acid: C 6 H 11 COOH: benzenecarboxylic acid: benzoic acid carboxybenzene dracylic acid: C 6 H 5 COOH: 2-hydroxybenzoic acid: salicylic acid: HOC 6 H 4 COOH: 2,2-dimethylpentanoic acid CH 3 (CH 2) 2 C(CH 3) 2 COOH 2,3-dimethylpentanoic acid C 2 H 5 (CHCH ...
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